List of variants reported as likely pathogenic for nonsyndromic genetic hearing loss by Laboratory of Medical Genetics, National & Kapodistrian University of Athens

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_004004.6(GJB2):c.-22-2A>C	rs201895089	0.00056
NM_000260.4(MYO7A):c.1829_1832dup (p.Ser611_Ser612insTer)	rs2135406725
NM_000260.4(MYO7A):c.517C>T (p.Gln173Ter)	rs782347270
NM_001854.4(COL11A1):c.3600+2T>C

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